Renal epithelial miR-205 expression correlates with disease severity in a mouse model of congenital obstructive nephropathy

Pediatr Res. 2016 Oct;80(4):602-9. doi: 10.1038/pr.2016.121. Epub 2016 Jun 7.

Abstract

Background: Congenital obstructive nephropathy (CON) is a leading cause of pediatric chronic kidney disease (CKD). Despite optimal surgical and medical care, there is a high rate of CKD progression. Better understanding of molecular and cellular changes is needed to facilitate development of improved biomarkers and novel therapeutic approaches in CON.

Methods: The megabladder (mgb) mouse is an animal model of CKD with impaired bladder emptying, hydronephrosis, and progressive renal injury. In this study, we characterize a particular microRNA, miR-205, whose expression changes with the degree of hydronephrosis in the mgb(-/-) kidney.

Results: Expression of miR-205 is progressively increased in the adult mgb(-/-) mouse with worsening severity of hydronephrosis. miR-205 expression is correlated with altered expression of cytokeratins and uroplakins, which are markers of cellular differentiation in urothelium. We describe the spatial pattern of miR-205 expression, including increased expression in renal urothelium and novel miR-205 expression in medullary collecting duct epithelium in the congenitally obstructed kidney.

Conclusion: miR-205 is increased with severity of CON and CKD in the mgb(-/-) mouse and may regulate urothelial differentiation.

Publication types

  • Research Support, N.I.H., Extramural

MeSH terms

  • Animals
  • Biomarkers / blood
  • Biomarkers / metabolism
  • Cell Differentiation
  • Disease Models, Animal
  • Disease Progression
  • Epithelium / metabolism*
  • Female
  • Gene Expression Regulation*
  • Hydronephrosis / blood
  • Keratins / blood
  • Kidney / metabolism
  • Kidney / pathology
  • Kidney Diseases / congenital*
  • Kidney Diseases / genetics
  • Kidney Diseases / physiopathology
  • Kidney Failure, Chronic / blood
  • Kidney Tubules, Collecting / metabolism
  • Male
  • Mice
  • Mice, Transgenic
  • MicroRNAs / genetics*
  • Tight Junctions
  • Uroplakins / blood
  • Urothelium / metabolism
  • Urothelium / pathology

Substances

  • Biomarkers
  • MIRN205 microRNA, mouse
  • MicroRNAs
  • Uroplakins
  • Keratins